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SCA13 (medical condition): A rare genetic disorder (chromosome 19 defect) characterized by...more »
SCA13 is listed as a "rare disease" by the Office of
Rare Diseases (ORD) of the National Institutes of Health
(NIH). This means that SCA13, or a subtype of SCA13,
affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)
SCA13: SCA13 is listed as a type of (or associated with) the following medical conditions in our database:
Some of the symptoms of SCA13 incude:
These medical disease topics may be related to SCA13:
Source - NIH
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